ZipRecruiter

Log In

1

Gmp Manufacturing Jobs (NOW HIRING)

Staffing

Be Seen First

Downstream GMP Manufacturing Associate

Rockville, MD · On-site

$20 - $23.49/hr

Downstream GMP Manufacturing Associate Site Location: Rockville, MD, 20850 Contract Duration: 3 months, 2 weeks, 3 days, Temp to possible perm Core hours M - F 8:30 am to 5 pm with flexible hours ...

New

Pace

PLS GMP Manufacturing Technician I

Norristown, PA · On-site

$22 - $28/hr

This is a full-time, onsite, GMP Manufacturing Technician (Solid Dose) position located in Norristown, PA,, Monday through Friday, 7:30 a.m. - 4:00 p.m. Compensation: $22.00 - $28.00 per hour The ...

Duke University

GMP Manufacturing Tech

Durham, NC · On-site

Duke University's Marcus Center for Cellular Cures (MC3) has a growth opportunity for a motivated individual to fill a GMP Manufacturing Technician in their Carolina Cord Blood Bank organization.

Buckeye Global IT Inc

Be Seen First

GMP MANUFACTURING ASSOCIATE - DOWNSTREAM

Rockville, MD · On-site

$22.50 - $23.50/hr

The Downstream GMP Manufacturing Associate will work as part of a team and work directly in activities associated with purification that applies a broad knowledge of biological, bioprocess, and ...

New

Duke University

GMP Manufacturing Tech

Durham, NC · On-site

Duke University's Marcus Center for Cellular Cures (MC3) has a growth opportunity for a motivated individual to fill a GMP Manufacturing Technician in their Carolina Cord Blood Bank organization.

Randstad

GMP Manufacturing Associate

Lexington, MA

$22 - $29/hr

Perform requests and execution of GMP documentation * Enter data in the Laboratory Information Management System (LIMS), MODA and or other business systems * Sample preparation and testing * Identify ...

next page

Showing results 1-20

All JobsGmp Manufacturing Jobs

Gmp Manufacturing information

See salary details

$13

$24

$34

How much do gmp manufacturing jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for gmp manufacturing in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $28.85 per hour, depending on experience, location, and employer.

What is a GMP manufacturing?

A GMP Manufacturing job involves producing pharmaceutical, biotechnology, or medical device products while following Good Manufacturing Practices (GMP) regulations. Responsibilities typically include operating equipment, maintaining sterile environments, documenting processes, and ensuring product quality and compliance. These roles are essential for maintaining safety and regulatory standards in healthcare-related manufacturing industries.

What are the key skills and qualifications needed to thrive in GMP manufacturing?

To excel in GMP Manufacturing, you need a solid understanding of Good Manufacturing Practices, attention to detail, and experience in regulated production environments, often backed by a degree in life sciences or engineering. Familiarity with quality management systems, batch record documentation, and equipment such as bioreactors or chromatography columns is typically required, and certifications like GMP or Six Sigma can be beneficial. Strong teamwork, communication skills, and the ability to follow precise procedures are essential soft skills for this position. These competencies ensure safe, compliant, and efficient production of pharmaceuticals or biotechnology products within strict regulatory frameworks.

What are some common challenges faced in GMP manufacturing roles?

Employees in GMP Manufacturing often encounter challenges such as maintaining meticulous documentation, adapting to changing regulatory requirements, and adhering to strict cleanliness and safety standards. The production process must be tightly controlled and deviations must be reported and resolved promptly, which requires a high level of diligence and accountability. Additionally, working collaboratively with quality assurance, engineering, and other cross-functional teams can add complexity to daily operations. Overcoming these challenges helps ensure product quality and regulatory compliance, while also providing valuable professional experience in one of the most highly regulated industries.

More about Gmp Manufacturing jobs
What cities are hiring for Gmp Manufacturing jobs? Cities with the most Gmp Manufacturing job openings:
What are the most commonly searched types of Gmp Manufacturing jobs? The most popular types of Gmp Manufacturing jobs are:
What states have the most Gmp Manufacturing jobs? States with the most job openings for Gmp Manufacturing jobs include:
What job categories do people searching Gmp Manufacturing jobs look for? The top searched job categories for Gmp Manufacturing jobs are:
Gmp Manufacturing jobs near you
Infographic showing various Gmp Manufacturing job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 4% Part Time, 1% Temporary, 4% Contract, and 3% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $51,890 per year, or $24.9 per hour.

GMP Manufacturing Documentation Specialist

Piper Companies

Ridgefield, NJ • On-site

$65 - $85/hr

Other

Posted 6 days ago

Job description

We are looking for an experienced GMP Manufacturing Documentation Specialist to support multiple sterile injectable technology transfer programs within a growing pharmaceutical manufacturing environment. This role is focused on authoring, revising, coordinating, and driving approval of GMP manufacturing documentation, with primary responsibility for Master Batch Records (MBRs) and related controlled manufacturing documents supporting Engineering, Media Simulation, Clinical, and PPQ manufacturing campaigns. This is fully on-site Monday-Friday in Ridgefield, New Jersey.
The ideal candidate will serve as a key partner to cross-functional Subject Matter Experts (SMEs), translating manufacturing processes into compliant GMP documentation while ensuring technical accuracy, document consistency, and timely approvals. This position is best suited for a professional with extensive sterile injectable manufacturing experience, strong GMP documentation expertise, and advanced Microsoft Word capabilities.
Key Responsibilities of the GMP Manufacturing Documentation Specialist:

  • Author, revise, and maintain GMP manufacturing documentation including Master Batch Records (MBRs), SOPs, forms, specifications, logbooks, and manufacturing instructions.
  • Collaborate with Manufacturing, Process Development, Quality, Validation, and other SMEs to gather and document technical process information.
  • Facilitate document review meetings, reconcile reviewer comments, resolve documentation discrepancies, and drive documentation through approval workflows.
  • Support documentation throughout Engineering, Media Simulation, Clinical, and PPQ manufacturing campaigns.
  • Convert validated manufacturing documentation into commercial Master Batch Records prior to transfer to Manufacturing Operations.
  • Ensure documents comply with applicable cGMP requirements, site procedures, Good Documentation Practices (GDP), and ALCOA+ Data Integrity principles.
  • Perform detailed proofreading and quality reviews to identify omissions, inconsistencies, formatting issues, and conflicting process information.
  • Track documentation status, review cycles, approvals, and project milestones while providing routine updates to project leadership.
  • Proactively identify documentation gaps, missing manufacturing instructions, inconsistent process parameters, and potential GMP documentation concerns, and work with SMEs to resolve them.
Qualifications of the GMP Manufacturing Documentation Specialist:
  • Bachelor's degree in a scientific, engineering, or related technical discipline, or an equivalent combination of pharmaceutical manufacturing and GMP documentation experience.
  • Minimum 5 years of experience supporting sterile injectable pharmaceutical manufacturing operations.
  • Minimum 3 years of demonstrated experience authoring and revising GMP Master Batch Records (MBRs) and manufacturing instructions.
  • Strong knowledge of current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and ALCOA+ Data Integrity principles.
  • Advanced proficiency in Microsoft Word, including complex formatting, tables, styles, templates, pagination, headers/footers, document editing, and tracked changes.
  • Demonstrated ability to critically review manufacturing documentation, identify technical and procedural gaps, and collaborate with SMEs to resolve issues.
  • Exceptional proofreading, organizational, and attention-to-detail skills.
  • Experience supporting sterile injectable technology transfer activities preferred.
Compensation & Benefits for the GMP Manufacturing Documentation Specialist:
  • Competitive hourly rate of $65-$85 per hour, commensurate with experience.
  • Opportunity to support high-visibility sterile injectable technology transfer and commercialization programs.
  • Work alongside cross-functional pharmaceutical manufacturing and technical operations teams.

Keywords: GMP Documentation, Master Batch Records, MBR Authoring, Sterile Injectables, Technology Transfer, Pharmaceutical Manufacturing, cGMP, GDP, ALCOA+, Manufacturing Instructions, PPQ, Aseptic Processing, Technical Writing, Validation Documentation, Microsoft Word
#LI-KI1 #LI-ONSITE
This job opens for applications on 07/19/2026. Applications for this job will be accepted for at least 30 days from the posting date.

Apply